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MEDGEARS,

⚠️ Moderate Risk

FEI: 3027265823 • New Delhi • INDIA

FEI

FEI Number

3027265823

📍

Location

New Delhi

🇮🇳

Country

INDIA
🏢

Address

Plot No 361 F/F Patparg, , New Delhi, , India

Moderate Risk

FDA Import Risk Assessment

33.5
LowModerateHighCritical

This firm has a moderate history of FDA import refusals. Some attention may be warranted.

Statistics

1
Total Refusals
2
Unique Violations
5/1/2024
Latest Refusal
5/1/2024
Earliest Refusal

Score Breakdown

Violation Severity
40.0×40%
Refusal Volume
11.2×30%
Recency
65.7×20%
Frequency
10.0×10%
How is this score calculated?

Proprietary Algorithm

  • 40% Violation Severity — AI-assessed (1-10)
  • 30% Refusal Volume — Logarithmic scale
  • 20% Recency — Decays over 5 years
  • 10% Frequency — Refusals per year

© ImportRefusal.com Original Analysis

Violation Summary

32801×

FRNMFGREG

The article is subject to refusal of admission pursuant to section 801(a)(3) in that it appears to be misbranded as defined in section 502(o) of the FD&C Act. It appears that it was manufactured, prepared, propagated, compounded, or processed in an establishment not duly registered under section 510 of the Act.

3411×

REGISTERED

It appears the device is subject to listing under 510(j) and the initial distributor has not registered as required by 21 CFR 807.20 (a)(5).

Refusal History

DateProductViolationsDivision
5/1/2024
89IMGSTIMULATOR, ULTRASOUND AND MUSCLE, FOR USE IN APPLYING THERAPEUTIC DEEP HEAT
3280FRNMFGREG
341REGISTERED
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is MEDGEARS,'s FDA import refusal history?

MEDGEARS, (FEI: 3027265823) has 1 FDA import refusal record(s) in our database, spanning from 5/1/2024 to 5/1/2024.

What is an FEI number?

FEI stands for Firm Establishment Identifier. It's a unique number assigned by the FDA to identify establishments that manufacture, process, pack, or hold food, drugs, medical devices, or other FDA-regulated products. MEDGEARS,'s FEI number is 3027265823.

What types of violations has MEDGEARS, received?

MEDGEARS, has been cited for 2 different violation type(s). Common FDA violations include adulteration (unsafe or unsanitary products), misbranding (incorrect or misleading labels), and regulatory non-compliance.

Where does this information about MEDGEARS, come from?

All FDA import refusal data for MEDGEARS, is sourced from the official FDA Data Dashboard (datadashboard.fda.gov), a public government database maintained by the U.S. Food and Drug Administration.

Data sourced from the FDA Data Dashboard, a public database maintained by the U.S. Food and Drug Administration.